10.1002/cssc.202002830
ChemSusChem
COMMUNICATION
potential to extend the tool-box and the scope of the
(de)hydrogenative transformations.
8525-8530; (l) M. Huang, Y. Li, Y. Li, J. Liu, S. Shu, Y. Liu, Z. Ke, Chem.
Commun. 2019, 55, 6213-6216; (m) M. Vellakkaran, K. Singh, D.
Banerjee, ACS Catal. 2017, 7, 8152-8158; (n) A. K. Bains, A. Kundu, S.
Yadav, D. Adhikari, ACS Catal. 2019, 9, 9051-9059.
Acknowledgements
[9] F. Kallmeier, R. Fertig, T. Irrgang, R. Kempe, Angew. Chem., Int. Ed.
2020, 59, 11789-11793.
We thank the NSFC (21673301, 21973113, and 21977019),
the Guangdong Natural Science Funds for Distinguished Young
Scholar (No. 2015A030306027), the Tip-top Youth Talents of
Guangdong Special Support Program (No.20153100042090537),
and the Fundamental Research Funds for the Central
Universities.
[10] (a) M. Peña-López, P. Piehl, S. Elangovan, H. Neumann, M. Beller,
Angew. Chem., Int. Ed. 2016, 55, 14967-14971; (b) U. K. Das, Y. Ben-
David, Y. Diskin-Posner, D. Milstein, Angew. Chem., Int. Ed. 2018, 57,
2179-2182; (c) Y. K. Jang, T. Krückel, M. Rueping, O. El-Sepelgy, Org.
Lett. 2018, 20, 7779-7783; (d) A. Kaithal, L.-L. Gracia, C. Camp, E. A.
Quadrelli, W. Leitner, J. Am. Chem. Soc. 2019, 141, 17487-17492; (e)
A. Kaithal, P. van Bonn, M. Hölscher, W. Leitner, Angew. Chem., Int. Ed.
2020, 59, 215-220; (f) M. Schlagbauer, F. Kallmeier, T. Irrgang, R.
Kempe, Angew. Chem., Int. Ed. 2020, 59, 1485-1490; (g) V. Yadav, V.
G. Landge, M. Subaramanian, E. Balaraman, ACS Catal. 2020, 10,
947-954.
Keywords: alcohol · borrowing hydrogen · outer-sphere
mechanism · tungsten · alkylation
[11] Y. Jing, Z. Ye, J. Su, Y. Feng, L.-B. Qu, Y. Liu, Z. Ke, Catal. Sci.
Technol. 2020, 10, 5443-5447.
[1] For selected examples and reviews: (a) A. J. A. Watson, J. M. J.
Williams, Science 2010, 329, 635-636; (b) C. Gunanathan, D. Milstein,
Science 2013, 341, 1229712; (c) X.-B. Lan, Z. Ye, M. Huang, J. Liu, Y.
Liu, Z. Ke, Org. Lett. 2019, 21, 8065-8070; (d) S. Thiyagarajan, C.
Gunanathan, J. Am. Chem. Soc. 2019, 141, 3822-3827; (e) X.-B. Lan, Z.
Ye, J. Liu, M. Huang, Y. Shao, X. Cai, Y. Liu, Z. Ke, ChemSusChem
2020, 13, 2557-2563; (f) A. Kumar, N. A. Espinosa-Jalapa, G. Leitus, Y.
Diskin-Posner, L. Avram, D. Milstein, Angew. Chem., Int. Ed. 2017, 56,
14992-14996; (g) S. Chakraborty, P. Daw, Y. Ben David, D. Milstein,
ACS Catal. 2018, 8, 10300-10305.
[12] (a) K.-T. Chan, T.-L. Lam, D. Yu, L. Du, D. L. Phillips, C.-L. Kwong, G.
S. M. Tong, G. Cheng, C.-M. Che, Angew. Chem., Int. Ed. 2019, 58,
14896-14900. (b) M. Montalti, A. Credi, L. Prodi, M. T. Gandolfi,
Handbook of Photochemistry, 3rd ed., CRC Press, Boca Raton, 2006,
pp. 619 – 623. (c) S. Li, D. P. Shelar, C.-C. Hou, Q.-Q. Chen, P. Deng,
Y. Chen, J. Photochem. Photobiol., A. 2018, 363, 44-50; (d) F. Raza, J.
H. Park, H.-R. Lee, H.-I. Kim, S.-J. Jeon, J.-H. Kim, ACS Catal. 2016, 6,
2754-2759.
[13] Q. Ye, Q. Wu, H. Zhao, Y.-M. Song, X. Xue, R.-G. Xiong, S.-M. Pang,
G.-H. Lee, J. Organomet. Chem. 2005, 690, 286-290.
[2] For selected reviews: (a) A. Corma, J. Navas, M. J. Sabater, Chem.
Rev. 2018, 118, 1410-1459; (b) T. Irrgang, R. Kempe, Chem. Rev. 2019,
119, 2524-2549; (c) G. A. Filonenko, R. van Putten, E. J. M. Hensen, E.
A. Pidko, Chem. Soc. Rev. 2018, 47, 1459-1483; (d) B. G. Reed-
Berendt, K. Polidano, L. C. Morrill, Org. Biomol. Chem. 2019, 17, 1595-
1607.
[14] W. W. Ellis, R. Ciancanelli, S. M. Miller, J. W. Raebiger, M. Rakowski
DuBois, D. L. DuBois, J. Am. Chem. Soc. 2003, 125, 12230-12236.
[3] L. Huang, M. Arndt, K. Gooßen, H. Heydt, L. J. Gooßen, Chem. Rev.
2015, 115, 2596-2697.
[4] For selected examples: (a) N. H. Park, E. V. Vinogradova, D. S. Surry,
S. L. Buchwald, Angew. Chem., Int. Ed. 2015, 54, 8259-8262; (b) P.
Ruiz-Castillo, S. L. Buchwald, Chem. Rev. 2016, 116, 12564-12649; (c)
X.-B. Lan, Y. Li, Y.-F. Li, D.-S. Shen, Z. Ke, F.-S. Liu, J. Org. Chem.
2017, 82, 2914-2925; (d) F.-Y. Zhang, X.-B. Lan, C. Xu, H.-G. Yao, T. Li,
F.-S. Liu, Org. Chem. Front. 2019, 6, 3292-3299.
[5] a) S. V. Ley, A. W. Thomas, Angew. Chem., Int. Ed. 2003, 42, 5400-
5449; b) E. Sperotto, G. P. M. van Klink, G. van Koten, J. G. de Vries,
Dalton Trans. 2010, 39, 10338-10351.
[6] Y. Watanabe, Y. Tsuji, Y. Ohsugi, Tetrahedron Lett. 1981, 22, 2667-
2670.
[7] For selected examples: (a) T. T. Dang, B. Ramalingam, S. P. Shan, A.
M. Seayad, ACS Catal. 2013, 3, 2536-2540; (b) M. Maji, K. Chakrabarti,
B. Paul, B. C. Roy, S. Kundu, Adv. Synth. Catal. 2018, 360, 722-729; (c)
R. Grigg, T. R. B. Mitchell, S. Sutthivaiyakit, N. Tongpenyai, J. Chem.
Soc., Chem. Commun. 1981, DOI: 10.1039/C39810000611, 611-612;
(d) M. Huang, Y. Li, J. Liu, X.-B. Lan, Y. Liu, C. Zhao, Z. Ke, Green
Chem. 2019, 21, 219-224; (e) S. N. R. Donthireddy, P. Mathoor Illam, A.
Rit, Inorg. Chem. 2020, 59, 1835-1847; (f) Y. Ai, P. Liu, R. Liang, Y. Liu,
F. Li, New J. Chem. 2019, 43, 10755-10762.
[8] For selected examples: (a) Y. Zhao, S. W. Foo, S. Saito, Angew. Chem.,
Int. Ed. 2011, 50, 3006-3009; (b) T. Yan, B. L. Feringa, K. Barta, Nat.
Commun. 2014, 5, 5602; (c) K. Polidano, B. D. W. Allen, J. M. J.
Williams, L. C. Morrill, ACS Catal. 2018, 8, 6440-6445; (d) A. Lator, S.
Gaillard, A. Poater, J. L. Renaud, Org. Lett. 2018, 20, 5985-5990; (e) S.
Rösler, M. Ertl, T. Irrgang, R. Kempe, Angew. Chem., Int. Ed. 2015, 54,
15046-15050; (f) M. Mastalir, G. Tomsu, E. Pittenauer, G. Allmaier, K.
Kirchner, Org. Lett. 2016, 18, 3462-3465; (g) G. Zhang, Z. Yin, S.
Zheng, Org. Lett. 2016, 18, 300-303; (h) S. P. Midya, J. Pitchaimani, V.
G. Landge, V. Madhu, E. Balaraman, Catal. Sci. Technol. 2018, 8,
3469-3473; (i) S. Elangovan, J. Neumann, J. B. Sortais, K. Junge, C.
Darcel, M. Beller, Nat. Commun. 2016, 7, 12641; (j) A. Mukherjee, A.
Nerush, G. Leitus, L. J. W. Shimon, Y. Ben David, N. A. Espinosa
Jalapa, D. Milstein, J. Am. Chem. Soc. 2016, 138, 4298-4301; (k) R.
Fertig, T. Irrgang, F. Freitag, J. Zander, R. Kempe, ACS Catal. 2018, 8,
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